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Total Synthesis of an Antifouling Marine Furanosesquiterpene

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Author(s)
Ungarean, Chad N.
Mason, Jeremy D.
Eyer, Benjamin R.
Duca, Nicholas S.
Mong, Jaimie M.
Murphree, S. Shaun
Date Issued
February 10, 2017
Abstract
An antifouling sesquiterpene isolated from Sinularia sp. was synthesized from citronellyl acetate in eight steps and 9% overall yield. The furan moiety was constructed using a multifunctional sulfone reagent.
Journal
Synthesis
Department
Chemistry
Citation
Ungarean, C.N., et al. (2017). Total Synthesis of an Antifouling Marine Furanosesquiterpene. Synthesis 49(10): 2177-2181. doi: 10.1055/s-0036-1588711.
Publisher
Thieme
Version of Article
Published article
Embargo
Post print of this article will be made available to the public after February 10, 2018.
DOI
10.1055/s-0036-1588711
ISSN
0039-7881
e1437-210X
Rights
Publisher's version can be used on author's personal website only. Post print can be used in a repository after a 12 month embargo.
Subjects

furans

sulfones

natural products

total synthesis

heterocycles

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